Clinical Research Coordinator - Turnhout

IQVIA Inc; Antwerpen; Hybrid; EUR 28,000 - 41,000; Part time

Job summary

IQVIA Belgium is seeking a Clinical Research Coordinator to support a Turnhout site on a part-time basis (8-10 hours per week). You will assist with prescreening, screening, data entry, and documentation, ensuring compliance with study protocols and regulatory requirements.

The role requires a life sciences background, at least 2 years at a clinical trial site, and strong organization and communication skills.

Qualifications

• Bachelor’s degree in life sciences or equivalent.
• Experience in clinical trials and study protocols.
• At least 2 years as CRA/Coordinator at a trial site.
• Excellent interpersonal and communication skills.
• Fluency in English.

Responsibilities

• Prescreening and screening tasks.
• Review charts from the site data base.
• Maintaining and updating study documentation (protocols, CRFs, EDC, eTMFs).
• Support patient screening and enrollment, including informed consent.

Skills

Clinical trials

IWRS experience

CRF familiarity

MS Office

Education

Bachelor’s degree in life sciences

Tools

MS Office

EDC systems

Job description

Clinical Research Coordinator - Turnhout### Clinical Research Coordinator - TurnhoutApply: Antwerp, Antwerp, Belgium: Part time: Posted Today: R1577435**Clinical Research Coordinator in Turnhout** **Working Hours:** 8-10 hours per week**Start Date**: Immediately **Duration**: Approximately 9 months IQVIA is currently recruiting a dedicated Clinical Research Coordinator to support a clinical research site in Turnhout. This **8-10 hour per week** role offers a unique opportunity to contribute to meaningful research in a collaborative and dynamic environment. **Key Responsibilities**As a vital member of the site team, you will help ensure the smooth execution of the clinical trial by performing a range of administrative and clinical support tasks, including:* Prescreening and Screening tasks* Review charts from the site data base* Maintaining and updating study documentation, including protocols, case report forms (CRFs), Electronic Data Capture (EDC) systems and eTMFs* Supporting patient screening and enrollment, including handling informed consent and privacy documentation* Lap sample processing and shipment* Use of IRT/IWRS systems for subject randomization, investigational product assignment, inventory management, and site-level clinical trial operations* Patient scheduling support* Coordinating logistical activities for study procedures in line with the study protocol* Communicating with study monitors and responding to study-related inquiries* Carrying out general administrative tasks related to the study **Your Profile** We are looking for candidates who bring a combination of education, experience, and skills:* Bachelor’s degree in life sciences or equivalent education and/or relevant experience in a clinical or medical setting (e.g., clinical research coordinator, research assistant, nurse, medical assistant)* Solid understanding of clinical trials and familiarity with study protocols, consent forms, and schedules* **Experience with lap samples and IRT/IWRS systems*** Good knowledge of medical terminology* Strong IT skills, including proficiency in MS Office applications (Outlook, Word, Excel, Access)* **Must have at least 2 years experience working as a Clinical Research Assistant, Research Nurse or Clinical Research Coordinator at a clinical trial site*** Excellent interpersonal and communication skills* Strong organizational skills and attention to detail* Fluency in English#LI-HCPN#LI-CES#LI-DNP#LI-NS#LI-OnsiteIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.comIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.